Canonical Allele Identifier: CA394798640

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-9938244-C-A
• MyVariant Identifiers: chr16:g.10032101C>A (hg19) ; chr16:g.9938244C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938244C>A , CM000678.2:g.9938244C>A	GRCh38
NC_000016.9:g.10032101C>A , CM000678.1:g.10032101C>A	GRCh37
NC_000016.8:g.9939602C>A	NCBI36
NG_011812.1:g.249511G>T
NG_011812.2:g.249511G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.722G>T MANE Select	ENSP00000332549.3:p.Ser241Ile
ENST00000535259.6:c.251G>T	ENSP00000441572.3:p.Ser84Ile
ENST00000636273.2:n.315G>T
ENST00000637393.1:c.314G>T	ENSP00000490232.1:p.Ser105Ile
ENST00000674742.1:c.251G>T	ENSP00000502200.1:p.Ser84Ile
ENST00000675189.1:n.1206G>T
ENST00000675398.1:c.722G>T	ENSP00000502752.1:p.Ser241Ile
ENST00000330684.3:c.722G>T	ENSP00000332549.3:p.Ser241Ile
ENST00000396573.6:c.722G>T	ENSP00000379818.2:p.Ser241Ile
ENST00000396575.6:c.311G>T	ENSP00000379820.3:p.Ser104Ile
ENST00000461292.3:n.361G>T
ENST00000535259.5:c.311G>T	ENSP00000441572.2:p.Ser104Ile
ENST00000562109.5:c.722G>T	ENSP00000454998.1:p.Ser241Ile
ENST00000566670.2:n.564G>T
ENST00000566683.1:n.241-47144G>T
ENST00000568247.3:n.614G>T
NM_000833.4:c.722G>T	NP_000824.1:p.Ser241Ile
NM_001134407.2:c.722G>T	NP_001127879.1:p.Ser241Ile
NM_001134408.2:c.722G>T	NP_001127880.1:p.Ser241Ile
XM_011522456.1:c.563G>T	XP_011520758.1:p.Ser188Ile
XM_011522457.1:c.464G>T	XP_011520759.1:p.Ser155Ile
XM_011522458.1:c.251G>T	XP_011520760.1:p.Ser84Ile
XM_011522459.1:c.251G>T	XP_011520761.1:p.Ser84Ile
XM_011522460.1:c.251G>T	XP_011520762.1:p.Ser84Ile
XM_011522461.1:c.722G>T	XP_011520763.1:p.Ser241Ile
XM_011522458.3:c.251G>T	XP_011520760.1:p.Ser84Ile
XM_011522461.3:c.722G>T	XP_011520763.1:p.Ser241Ile
XM_017023172.1:c.878G>T	XP_016878661.1:p.Ser293Ile
XM_017023173.1:c.878G>T	XP_016878662.1:p.Ser293Ile
NM_001134407.3:c.722G>T MANE Select	NP_001127879.1:p.Ser241Ile
NM_000833.5:c.722G>T	NP_000824.1:p.Ser241Ile